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1.
Neurocase ; 28(3): 263-269, 2022 06.
Article in English | MEDLINE | ID: mdl-35695794

ABSTRACT

Prosopamnesia is a face-selective memory disorder in which face learning is impaired, while face-perception disorder (prosopagnosia) and memory disorders for stimuli other than faces are not present. To date, only two cases of prosopamnesia have been reported in adults - one congenital and one secondary to brain damage. This article reports a case of a 68-year-old woman complaining difficulties recognizing persons she had got to know recently. Neuropsychological examination revealed face-specific anterograde amnesia in the absence of prosopagnosia and other memory impairments. Brain MRI did not present any focal abnormality; PET-scan revealed hypoactivation mostly in the frontotemporal area bilaterally. This patient represents the first case of late-onset primary prosopamnesia.


Subject(s)
Prosopagnosia , Adult , Aged , Amnesia/etiology , Face , Female , Humans , Memory Disorders , Neuropsychological Tests , Pattern Recognition, Visual/physiology , Prosopagnosia/diagnosis , Prosopagnosia/etiology
2.
Clin Neuropsychol ; 36(8): 2370-2378, 2022 11.
Article in English | MEDLINE | ID: mdl-34459356

ABSTRACT

OBJECTIVE: Boucher-Neuhäuser Syndrome (BNS) is a rare autosomal recessive disorder characterized by hypogonadotropic hypogonadism, spinocerebellar ataxia, and chorioretinal syndrome, and associated with a variant in the PNPLA6 gene. Although many reports have mentioned the presence of cognitive impairment, a neuropsychological assessment of a BNS case has never been published. Here, we provide a detailed description of a young adult patient with BNS who has a homozygous pathogenic variant in the PNPLA6 gene. METHOD: A 21-year-old man with progressive ataxia and a history of hypogonadotropic hypogonadism and chorioretinal dystrophy was diagnosed with BNS. A comprehensive cognitive evaluation was performed, requiring the ad hoc selection and adaption of neuropsychological tests to overcome visual and motor impairments that characterize this syndrome. RESULTS: The patient presented an intact global cognitive profile with selective executive dysfunction and mild verbal reasoning dysfunction. In particular, attentional-inhibitory control, working memory, and set switching were impaired, and inadequate development of conceptual knowledge and abstract reasoning was observed. CONCLUSIONS: This is the first report of an explicitly documented comprehensive neuropsychological assessment in a patient with BNS. The battery we composed is an example of a methodology that can be used to conduct a detailed cognitive examination without being penalized for physical impairment.Further studies are needed to define the typical cognitive features that characterize BNS and possibly identify its cognitive phenotype(s).


Subject(s)
Hypogonadism , Spinocerebellar Ataxias , Humans , Hypogonadism/complications , Hypogonadism/diagnosis , Hypogonadism/genetics , Mutation , Neuropsychological Tests , Phospholipases/genetics , Spinocerebellar Ataxias/complications , Spinocerebellar Ataxias/diagnosis , Spinocerebellar Ataxias/genetics
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